Canonical Allele Identifier: CA1167798613

Gene: FAM151A ACOT11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54609716_54609731delinsAAGAGGCCAAGGCTGG , CM000663.2:g.54609716_54609731delinsAAGAGGCCAAGGCTGG	GRCh38
NC_000001.10:g.55075389_55075404delinsAAGAGGCCAAGGCTGG , CM000663.1:g.55075389_55075404delinsAAGAGGCCAAGGCTGG	GRCh37
NC_000001.9:g.54847977_54847992delinsAAGAGGCCAAGGCTGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302250.7:c.1295_1310delinsCCAGCCTTGGCCTCTT (FAM151A) MANE Select	ENSP00000306888.2:p.Ser432=
ENST00000343744.7:c.*604_*619delinsAAGAGGCCAAGGCTGG (ACOT11) MANE Select	ENSP00000340260.2:n.*604_*619delinsAAGAGGCCAAGGCTGG
ENST00000302250.6:c.1295_1310delinsCCAGCCTTGGCCTCTT (FAM151A)	ENSP00000306888.2:p.Ser432=
ENST00000343744.6:c.*604_*619delinsAAGAGGCCAAGGCTGG (ACOT11)	ENSP00000340260.2:n.*604_*619delinsAAGAGGCCAAGGCTGG
ENST00000371304.2:c.918-184_918-169delinsCCAGCCTTGGCCTCTT (FAM151A)	ENSP00000360353.2:n.918-184_918-169delinsCCAGCCTTGGCCTCTT
ENST00000371316.3:c.1629+1648_1629+1663delinsAAGAGGCCAAGGCTGG (ACOT11)	ENSP00000360366.3:n.1629+1648_1629+1663delinsAAGAGGCCAAGGCTGG...
ENST00000481208.5:n.2467_2482delinsAAGAGGCCAAGGCTGG (ACOT11)
NM_015547.3:c.1629+1648_1629+1663delinsAAGAGGCCAAGGCTGG (ACOT11)	NP_056362.1:n.1629+1648_1629+1663delinsAAGAGGCCAAGGCTGG
NM_147161.3:c.*604_*619delinsAAGAGGCCAAGGCTGG (ACOT11)	NP_671517.1:n.*604_*619delinsAAGAGGCCAAGGCTGG
NM_176782.2:c.1295_1310delinsCCAGCCTTGGCCTCTT (FAM151A)	NP_788954.2:p.Ser432=
XM_006710599.2:c.1217_1232delinsCCAGCCTTGGCCTCTT (FAM151A)	XP_006710662.1:p.Ser406=
XM_006710599.3:c.1217_1232delinsCCAGCCTTGGCCTCTT (FAM151A)	XP_006710662.1:p.Ser406=
NM_176782.3:c.1295_1310delinsCCAGCCTTGGCCTCTT (FAM151A) MANE Select	NP_788954.2:p.Ser432=
NM_015547.4:c.1629+1648_1629+1663delinsAAGAGGCCAAGGCTGG (ACOT11)	NP_056362.1:n.1629+1648_1629+1663delinsAAGAGGCCAAGGCTGG
NM_147161.4:c.*604_*619delinsAAGAGGCCAAGGCTGG (ACOT11) MANE Select	NP_671517.1:n.*604_*619delinsAAGAGGCCAAGGCTGG